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首页> 外文期刊>Amyotrophic lateral sclerosis eofficial publication of the World Federation of Neurology Research Group on Motor Neuron Diseases >Elevated CSF TDP-43 levels in amyotrophic lateral sclerosis: Specificity, sensitivity, and a possible prognostic value
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Elevated CSF TDP-43 levels in amyotrophic lateral sclerosis: Specificity, sensitivity, and a possible prognostic value

机译:肌萎缩性侧索硬化症中CSF TDP-43水平升高:特异性,敏感性和可能的​​预后价值

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摘要

TAR DNA binding protein of 43 kDa (TDP-43) is likely to be the major pathogenetic protein in amyotrophic lateral sclerosis (ALS). A previous study has shown that levels of TDP-43 in CSF measured by an ELISA are significantly higher for ALS patients than for controls. The aim of this study was to investigate whether elevated CSF TDP-43 levels are specific to ALS, and are associated with clinical profiles in ALS patients. We measured CSF TDP-43 levels by the same ELISA in 27 ALS patients and 50 neurodegenerative or inflammatory disease controls such as Parkinson's disease, multiple sclerosis, and Guillain-Barré syndrome. Results showed that the CSF TDP-43 levels were increased only in ALS patients. Receiver operating characteristic (ROC) analyses showed a sensitivity of 59.3% and a specificity of 96.0%. We also found that lower CSF TDP-43 levels may be associated with shorter survival time. In conclusion, the CSF TDP-43 is a potential biomarker that supports a diagnosis of ALS. Moreover, among ALS patients, lower levels of CSF TDP-43 may reflect the accumulation of TDP-43 in the cortical and spinal motor neurons and thereby shorter survival time, although this should be confirmed in larger prospective studies.
机译:43 kDa的TAR DNA结合蛋白(TDP-43)可能是肌萎缩性侧索硬化症(ALS)的主要致病蛋白。先前的研究表明,通过ELISA测定的ALS患者的CSF中TDP-43的水平明显高于对照组。这项研究的目的是调查升高的CSF TDP-43水平是否对ALS具有特异性,并且与ALS患者的临床特征有关。我们通过相同的ELISA方法在27位ALS患者和50位神经退行性或炎性疾病对照(如帕金森氏病,多发性硬化症和格林-巴利综合征)中测量了CSF TDP-43水平。结果显示,仅在ALS患者中CSF​​ TDP-43水平升高。接收器工作特性(ROC)分析显示灵敏度为59.3%,特异性为96.0%。我们还发现较低的CSF TDP-43水平可能与较短的生存时间有关。总之,CSF TDP-43是支持ALS诊断的潜在生物标志物。此外,在ALS患者中,较低的CSF TDP-43水平可能反映了TDP-43在皮质和脊髓运动神经元中的积累,从而缩短了生存时间,尽管这在较大的前瞻性研究中应得到证实。

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